• Electrical SME Engineering

    Merck (Durham, NC)
    …Vaccine Technology (GVTE), Automation, and Quality approvers. + Perform a thorough review of design & engineering records and related Good Manufacturing Practices ... in a timely manner, and implementing corrective actions to improve the execution/ review process for equipment. + Develop training material. Working as a subject… more
    Merck (08/16/25)
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  • Supervisory Control Specialist

    Wells Fargo (Greenville, NC)
    …and consult regarding policies and procedures, controls, tools and training + Review and analyze controls to manage high risk investment strategies and complex ... through meaningful statistics + Develop expertise in firm, compliance and regulatory policies and procedures + Collaborate and consult with Financial Advisors,… more
    Wells Fargo (08/13/25)
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  • Qualified Professional-Clinical Supervisor (Afl)

    BrightSpring Health Services (Charlotte, NC)
    …within general resource and reimbursement models. Ensures compliance with regulatory requirements, including the proper delivery and documentation of services ... in ISP development or develops ISP/PCP/care plans + Monthly and quarterly review and documentation of individuals' progress + Demonstrates knowledge of and monitors… more
    BrightSpring Health Services (08/12/25)
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  • Legal Counsel

    Coinbase (Raleigh, NC)
    …products. We're looking for a lawyer with solid product development, regulatory and negotiation skills preferably developed within the traditional derivatives, ... Stay abreast of and advise on digital currency and blockchain technology legal and regulatory issues, particularly in the US, UK, EU and elsewhere. * Lead and assist… more
    Coinbase (08/09/25)
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  • Senior Counsel (Medical Device)

    Fujifilm (Raleigh, NC)
    …advertising and marketing, competitor interactions, and other matters. + Draft, review and negotiate a variety of complex commercial contracts, including customer, ... colleagues and outside counsel on a regular basis to review and handle a large volume of contracts, to...Counsel and senior business management on general legal and regulatory risks affecting the Medical Device businesses, including with… more
    Fujifilm (08/08/25)
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  • CSV Automation Engineer

    J&J Family of Companies (Wilson, NC)
    …points of the computerized system lifecycle, ensuring compliance with regulatory requirements, Computer Systems Validation (CSV) and Lifecycle procedures with ... automation systems compliance current Good Manufacturing Practices (cGMPs) and all other regulatory and/or guidance requirements such as Annex 11, GAMP and 21 CFR… more
    J&J Family of Companies (08/16/25)
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  • Chief Medical Officer

    LifePoint Health (Henderson, NC)
    …safe patient care. Regularly meet with CMO of Duke LifePoint to review initiatives and discuss opportunities for improvement. Actively engaged in antibiotic ... CMO of LifePoint Health. Assist hospital in assuring compliance with standards of regulatory agencies. Assist with surveys and issues related to The Joint Commission… more
    LifePoint Health (08/09/25)
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  • Assistant General Counsel - Nuclear & Precision…

    Cardinal Health (Raleigh, NC)
    …to commercial, corporate securities, intellectual property, labor and employment, and regulatory law, among other areas. This function also litigates all company ... (GPOs, IDNs, hospitals, physician offices, etc.), strategic sourcing, marketing, regulatory /compliance and contract manufacturing. **_Responsibilities_** + Demonstrate strong business… more
    Cardinal Health (08/02/25)
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  • Senior Staff Quality Specialist

    GRAIL (Durham, NC)
    …not limited to all-Quality, Clinical Laboratory Operations,Technical Operations, Regulatory Affairs, Compliance, Program Management, Clinical Affairs, Supply Chain, ... concepts and principles in accordance with GRAIL's quality management system and regulatory requirements including ISO 13485, ISO 14971, 21 CFR 820, IVDR,… more
    GRAIL (07/26/25)
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  • Associate Director, MSAT, Downstream Drug…

    Otsuka America Pharmaceutical Inc. (Raleigh, NC)
    …aspects of downstream process technology transfers to CDMOs, including documentation review , gap analysis, and risk assessment. + Provide expert technical oversight ... of downstream manufacturing operations at CDMOs, including review of batch records, deviation investigations, and change controls. + Lead or significantly contribute… more
    Otsuka America Pharmaceutical Inc. (07/18/25)
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